Heparan Sulfate, Mucopolysaccharidosis IIIB and Sulfur Metabolism Disorders

Mucopolysaccharidosis, type IIIB (MPS IIIB) is a rare disease caused by mutations in the N-alpha-acetylglucosaminidase (NAGLU) gene resulting in decreased or absent enzyme activity. On the cellular level, the disorder is characterized by the massive lysosomal storage of heparan sulfate (HS)—one spec...

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Detalles Bibliográficos
Autores principales: Kaczor-Kamińska, Marta, Kamiński, Kamil, Wróbel, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9026333/
https://www.ncbi.nlm.nih.gov/pubmed/35453363
http://dx.doi.org/10.3390/antiox11040678

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9026333/
https://www.ncbi.nlm.nih.gov/pubmed/35453363
http://dx.doi.org/10.3390/antiox11040678

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